Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP888433.RAA7RQoeu_TF9_101B7ECHg4Cmque42V0_V15x4XNuuio130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP888433.RAA7RQoeu_TF9_101B7ECHg4Cmque42V0_V15x4XNuuio130_provenance.
• NP637701.RAXCOq4c2ueckoJmj7r_9TjfhNVbG-2KYrCmnF7S9b6W0130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP637701.RAXCOq4c2ueckoJmj7r_9TjfhNVbG-2KYrCmnF7S9b6W0130_provenance.
• NP367321.RAolBdR-6wQuQj-Ono5UnmUIBsr6uXv-WJtIWdP8XKQPU130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367321.RAolBdR-6wQuQj-Ono5UnmUIBsr6uXv-WJtIWdP8XKQPU130_provenance.
• NP650860.RAlqR3CIiTgEJmZfZScrx_6bMsW86i39SLoGWgcIkC9xA130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650860.RAlqR3CIiTgEJmZfZScrx_6bMsW86i39SLoGWgcIkC9xA130_provenance.
• NP528963.RAw1CxbtLcHYcEZcchPxIKQsA62_qgqR5cCkkAr6IzV1U130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528963.RAw1CxbtLcHYcEZcchPxIKQsA62_qgqR5cCkkAr6IzV1U130_provenance.
• NP835962.RAQs5icZ4SBdejReJ_gpQGYfuLoh6Fbh5QGzs5rF7ktZc130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835962.RAQs5icZ4SBdejReJ_gpQGYfuLoh6Fbh5QGzs5rF7ktZc130_provenance.
• NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805067.RA6pjhnWZCxtIdg4NhxP8SoKIfYsCI_vAvmnmyFMmncgs130_provenance.
• NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437106.RAaHNm_nVcyGnkp4IZF4xTYmmKEWzKK0n1FHFiTFKZTmE130_provenance.
• NP647338.RAeh2l-ugnWlS9K-jpftVLcwMHqGhu-9OjBqssrCpQQH0130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647338.RAeh2l-ugnWlS9K-jpftVLcwMHqGhu-9OjBqssrCpQQH0130_provenance.
• NP647517.RAS7j3Fi69C8LX29qRKKGkC2bXrIPXLUFpzwz_yx4l4Ro130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647517.RAS7j3Fi69C8LX29qRKKGkC2bXrIPXLUFpzwz_yx4l4Ro130_provenance.
• NP598783.RAL10RCDE0EDJcVPSMvfUJrecF1YYnbblEYZU-I3EGfCM130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598783.RAL10RCDE0EDJcVPSMvfUJrecF1YYnbblEYZU-I3EGfCM130_provenance.
• assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1354702.RAWJT3peK0MACLTxv2AMDLNXEN4PPlPLVrrbkWKh4woZY130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354702.RAWJT3peK0MACLTxv2AMDLNXEN4PPlPLVrrbkWKh4woZY130_provenance.
• NP1354703.RAcG16Cenz-AWM4KQyoFQ2Q8sGQ-EoAawJrJayBiRtvlk130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354703.RAcG16Cenz-AWM4KQyoFQ2Q8sGQ-EoAawJrJayBiRtvlk130_provenance.
• NP1354705.RAWYE-90alvUkbcoxvajyJXClzeonz-j7xThJZnA2vk50130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354705.RAWYE-90alvUkbcoxvajyJXClzeonz-j7xThJZnA2vk50130_provenance.
• NP1354707.RASMiWd1cOG_7hV-vlCyeM7MMmpHLNuUGMUCmT9sYT78k130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354707.RASMiWd1cOG_7hV-vlCyeM7MMmpHLNuUGMUCmT9sYT78k130_provenance.
• NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437090.RAukW_eCTtuxmGcNXsv9m43S1JgMLOJb-0PRn_vSZPKNA130_provenance.
• NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437094.RAmjj6gQRvo26hF6bOF5HxfuiAV-wuUbWVX01JoqE6fYg130_provenance.
• NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354709.RAAXpA-s4A0uWjnHk5ueSr5p0uUlYc4YYx2SlsBA7H19A130_provenance.
• NP437113.RA2KdqZoMjKMDzXrsh18mfyf9pULoI8Fy5jZszOvaNlQE130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP437113.RA2KdqZoMjKMDzXrsh18mfyf9pULoI8Fy5jZszOvaNlQE130_provenance.
• NP1354712.RAJmz6U29qxsv7epOfJLSC6g9jI29nz7750sXczHrHbgQ130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354712.RAJmz6U29qxsv7epOfJLSC6g9jI29nz7750sXczHrHbgQ130_provenance.
• NP1354710.RA3pGLvMxRZ9cngPD2NNKBlP6qDzFXmHYlLKhhAMeUFi4130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354710.RA3pGLvMxRZ9cngPD2NNKBlP6qDzFXmHYlLKhhAMeUFi4130_provenance.
• NP1354711.RA7zcZXKUAU9xzpJOJVq1pM2cQI-HDt98sEyx-FRlL62w130_assertion description "[GSS and PrP-CAA are associated with point mutations of the prion protein gene (PRNP); these conditions show a broad spectrum of clinical presentation, the main signs being ataxia, spastic paraparesis, extrapyramidal signs and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1354711.RA7zcZXKUAU9xzpJOJVq1pM2cQI-HDt98sEyx-FRlL62w130_provenance.